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MI Product Line

FDA UDI

Class I (US FDA UDI)

by Medical Illumination International, Inc

Identity

Trade Name
MI Product Line FDA UDI
Generic Name
Medical monitor/light mount FDA UDI
Device Name
MI-500 Examination Light, Wall Mount FDA UDI
Model / Reference
061312 FDA UDI
Description
MI-500 Examination Light, Wall Mount FDA UDI

Identifiers

Primary DI / UDI-DI
00816835020096 FDA UDI
FDA Product Code
KZF FDA UDI
GMDN Term
Medical monitor/light mount FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6320 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Operating room lightMedical monitor/light mount

MI Product Line by Medical Illumination International, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical monitor/light mount.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 14c14906-4dbf-4e16-bab3-f156055e44d1 33 fields · synced Jun 8, 2026